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FDA Import Refusal 101-6222966-0/11/1 — Dornier Medtech GmbH

Dornier Medtech GmbH — FEI 3002806833

The FDA refused shipment 101-6222966-0/11/1 from Dornier Medtech GmbH (Germany) on October 21, 2019. The refused product falls under Devices — POWERED LASER SURGICAL INSTRUMENTS. Cited charges: 118,476,508 This firm has 2 other import refusals on record.

Refusal Details

Date
October 21, 2019
Country
Germany
Product Category
Devices
Product Code
79GEX POWERED LASER SURGICAL INSTRUMENTS
Charges
118,476,508

Recent inspections

  • 1194137 (NAI Wed Dec 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 726892 (OAI Fri Apr 29 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

Other import refusals

  • 101-6222966-0/21/1 (Mon Oct 21 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • DM9-0100527-0/1/1 (Mon Jan 07 2002 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources